Homozygous calreticulin mutations in patients with myelofibrosis lead to acquired myeloperoxidase deficiency

Autor: Theocharides, Alexandre P.A., Lundberg, Pontus *, Lakkaraju, Asvin K.K. *, Lysenko, Veronika, Myburgh, Renier, Aguzzi, Adriano, Skoda, Radek C., Manz, Markus G.
Zdroj: In Blood 23 June 2016 127(25):3253-3259
Databáze: ScienceDirect